Courtney Caputo Appointed as Chair of the National Board
The Epilepsy Foundation of America is excited to announce Courtney Caputo's appointment as Chair of the National Board of Directors. Her journey with epilepsy and extensive experience in advocacy make her a perfect fit for this critical role at a pivotal moment for the Foundation.
Caputo's Advocacy Work and Personal Connection
Caputo has been a steadfast advocate for the epilepsy community for many years. She founded "Team Super T", a leading fundraising team for walks dedicated to raising awareness and support for epilepsy. This initiative is named in honor of her daughter, who also lives with the condition. Additionally, Caputo serves as Chair of the National Epilepsy Walk and has previously occupied various leadership positions within the Foundation, including Vice Chair.
Impact on National Advocacy
Her advocacy is rooted in personal experience, as she deeply understands the complexities of epilepsy. "What inspired me to become an advocate is the complexity of this disease," Caputo shared. "It is my mission to be a guiding resource for families facing the everyday challenges of epilepsy."
Professional Background
In her professional sphere, Caputo is the Senior Vice President of Global Government Relations at Parsons Corporation. In this position, she effectively represents the interests of 19,000 employees and oversees operations generating more than $5 billion in revenue each year, supporting defense and critical infrastructure initiatives. Her leadership has resulted in significant business growth, with more than $250 million driven yearly in various sectors.
Previous Experience
Her career also includes pivotal roles at Raytheon Technologies, where she played a crucial part in business development and government relations. Caputo's expertise was honed through her strategic consulting at Michael E. Dunn & Associates, and her public policy work at Deloitte. She also has congressional experience working with a U.S. Representative.
Foundation Priorities Under Caputo's Leadership
Caputo's vision for her term as Chair includes a strong focus on enhancing education, policy reform, research funding, and combatting stigma associated with epilepsy. She emphasized the importance of building relationships to strengthen research and medical funding, saying, "It’s an honor to lead the Board in this crucial work for all families affected by epilepsy."
About Epilepsy
With nearly 3.4 million Americans affected by epilepsy, the condition is recognized as the most prevalent chronic brain disorder globally. It is characterized by recurring seizures, which arise from sudden electrical disruptions in the brain, leading to various behavioral, awareness, and bodily control challenges. The impacts of epilepsy extend beyond the seizures themselves, negatively affecting memory, mood, and concentration.
About the Epilepsy Foundation of America
The Epilepsy Foundation is a dedicated nonprofit organization devoted to improving the lives of people touched by epilepsy through education, advocacy, and funding. With over five decades of commitment, the Foundation focuses on raising awareness, reducing stigma, and supporting strategies that facilitate significant advancements for those living with epilepsy. Their mission includes funding innovative research and supporting new investigators working on treatments and therapies. The Foundation also enhances access to care and training in seizure recognition.
Get in Touch with the Foundation
If you wish to learn more, please contact Kaitlyn Gallagher at 301.918.3756 or via email at kgallagher@efa.org.
Frequently Asked Questions
Who is Courtney Caputo?
Courtney Caputo is the newly appointed Chair of the National Board of Directors for the Epilepsy Foundation of America and an advocate for the epilepsy community.
What does her role involve?
As Chair, Caputo will lead the Board in strategic initiatives focused on education, policy reform, research funding, and stigma reduction.
What is Team Super T?
Team Super T is a fundraising team dedicated to supporting epilepsy initiatives, founded by Caputo in honor of her daughter living with epilepsy.
How can I contact the Epilepsy Foundation?
You can reach out through the provided media contact, Kaitlyn Gallagher, at 301.918.3756 or via email at kgallagher@efa.org.
What is the mission of the Epilepsy Foundation?
The Foundation is committed to improving the lives of those affected by epilepsy through education, research, and advocacy efforts.
